Our Team

As Co-Founder of AQniX Research Solutions, he leads the organization with a strategic vision focused on quality, compliance, and innovation. He oversees the development of inspection-ready systems, custom digital QA tools, and regulatory-aligned services tailored for CROs, sponsors, and academic institutions. His leadership reflects a unique blend of scientific depth, regulatory insight, and technological foresight, fostering AQniX’s reputation as a forward-thinking partner in clinical research. Under his guidance, AQniX continues to deliver high-impact, compliant, and scalable solutions to meet the evolving demands of the global clinical research industry.

PROFESSIONAL EXPERIENCE:
He has played pivotal roles in renowned organizations such as HeaDS Research (Europe), Veeda Lifesciences Ltd., Axis Clinical Ltd., Lambda Therapeutics Ltd., Cliantha Research Ltd., and Wockhardt Research Centre. He has conducted and overseen 300+ audits, including international on-site audits in Switzerland, Greece, Italy, Czech Republic, and Turkey. He has led, supported, and executed over 350+ clinical trials, including BA/BE studies and Phase I, patient-based PK trials, and late-phase trials across various therapeutic areas such as cardiology, oncology, pulmonology, neurology, and psychiatry. His audit scope has encompassed study audits, vendor assessments, system audits, and regulatory inspections. His in-depth engagement with global health authorities — including USFDA, WHO, ANVISA, CDSCO, EMEA, MHRA, NPRA (Malaysia), Kazakhstan, and GCC regulators — reflects his strong command of international compliance standards.

SPECIALIZED EXPERTISE:
His expertise lies in designing and implementing Quality Management Systems (QMS) tailored to clinical trial environments, including SOP development, documentation control, and GCP-compliant frameworks. His technical capabilities span SAS programming, data management, and validated statistical workflows, supporting BA/BE and PK studies. He has also been instrumental in software validation, contributing to the development, design, and testing of platforms like eCRF, eTMF, QMS, RDMT, and DMS, thereby enhancing efficiency and regulatory alignment. His skill set integrates scientific rigor, regulatory knowledge, and digital innovation, making him a key driver in transforming clinical operations.

As Co-Founder of AQniX Research Solutions, he provides strategic, technical, and operational leadership. He plays a central role in developing inspection-ready systems, implementing custom digital QMS tools, and offering regulatory-aligned services to CROs, sponsors, and academic institutions. his leadership is defined by a unique blend of innovation, quality focus, and regulatory expertise. Under his guidance, AQniX continues to build a reputation for delivering high-impact, scalable, and compliant solutions that meet the evolving demands of the global clinical research industry.

PROFESSIONAL EXPERIENCE:
He is the strategic force behind AQniX Research Solutions, bringing over a decade of specialized experience in clinical research, regulatory compliance, and quality systems development. His professional journey spans leadership roles at reputed organizations across India such as Veeda Lifesciences, Axis Clinical Limited, Raptim Research Pvt. Ltd., and Enem Nostrum Remedies Pvt. Ltd. He has successfully led and supported 200+ clinical studies across India in diverse domains including BA/BE trials, pharmacokinetic (PK) studies, late-phase trials, and pediatric/infant research, with therapeutic expertise covering oncology, psychiatry,gastroenterology, ophthalmology, and dermatology.

With a robust command over quality frameworks and regulatory operations, he has conducted or facilitated 250+internal and external audits, including 50+ vendor audits, all aligned with NABL and CAP. He has worked inclose coordination with leading global regulatory authorities such as DCGI, USFDA, EMA, ANVISA, and MHRA, consistently demonstrating adherence to international standards and reinforcing a culture of quality, compliance, and scientific integrity.

SPECIALIZED EXPERTISE:
His core strengths lie in building and implementing robust Quality Management Systems (QMS), as well asin clinical data management and software validation. He has extensive experience with platforms such as EDC, eTMF, CTMS, QMS, and DMS, contributing to enhanced accuracy, compliance, and system integration across clinical operations. he is known for his technical problem-solving skills and process optimization strategies and has designed various tech-driven solutions to streamline interdepartmental performance. His integrated approach has consistently improved efficiency and regulatory compliance across organizational levels.

As Co-founder of AQniX Research Solutions, she plays a pivotal role in driving the company’s strategic and technical direction. She has led the integration of AI-based CTMS platforms, established quality-centric workflows, and helped forge global partnerships aimed at expanding AQniX service capabilities. Her leadership style is innovation-driven, process-focused, and deeply rooted in compliance, helping position AQniX as a trusted partner in clinical research. With a focus on efficiency, transparency, and data-driven decision-making and continues to champion the company’s mission of delivering excellence in clinical innovation.

PROFESSIONAL EXPERIENCE:
Throughout her illustrious career, she has held pivotal leadership positions at some of the most respected institutions in clinical research, including Radiance Hospital, Veeda Lifesciences, and Synchron Research. In each of these esteemed organizations, she has demonstrated exceptional acumen in operational leadership, strategic execution, and the development of robust quality systems. Renowned for her unwavering commitment to excellence, she has played a transformative role in the successful execution of complex clinical trials particularly in the critical therapeutic area of Neurology, Oncology, psychiatry, gastrointestinal, ophthalmology, dermatology and Immunosuppressant ensuring full alignment with stringent global regulatory standards. Her expertise extends far beyond trial management; she has consistently pioneered operational frameworks that elevate compliance, drive innovation, and set new benchmarks for quality in clinical research.

With a proven track record of delivering impactful outcomes in highly regulated and high-stakes environments, she continues to be a force of vision and precision, seamlessly integrating scientific integrity with operational excellence at every stage of clinical development.

SPECIALIZED EXPERTISE:
She core strengths lie in Quality Management Systems (QMS), clinical data integrity, data management, and process optimization. She has demonstrated expertise in using clinical technologies such as CTMS, eCRF, DMS, PheeDIt, and Clinion, and has developed tools and processes that streamline data capture and reporting. A key innovation she led was the design of a proprietary risk-based monitoring system, aimed at improving efficiency and quality in clinical oversight. Her approach to documentation, SOP compliance, and system integration reflects her commitment to operational excellence and audit-readiness.